Adverse Drug Event Reporting System

**Semantic type:** Intellectual Product

**Definition:** A Web application developed for the electronic submission of Expedited Reports to the NCI for serious and/or unexpected Adverse Events, deaths, and other events defined in the NCI Guidelines: Adverse Event Reporting Requirements for NCI Investigational Agents

**Synonyms:** - AdEERS - Adverse Drug Experience Reporting System - Adverse Event Expedited Reporting System - Adverse Event Reporting System - CTEP AERS - CTEP Adverse Event Reporting System - Cancer Therapy Evaluation Program Adverse Event Reporting System